Variant report

Variant	nsv874472
Chromosome Location	chr2:86961252-87071474
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1424)
CpG islands
(count:3120)
Chromatin interactive
region (count:43)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:9)

(count:1424 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:87062188-87062388	K562	blood:	n/a	n/a
2	ARID3A	chr2:87035044-87036047	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:87035534-87035903	K562	blood:	n/a	n/a
4	ARID3A	chr2:86975391-86975453	K562	blood:	n/a	n/a
5	ATF1	chr2:86975197-86975467	K562	blood:	n/a	n/a
6	ATF1	chr2:87064398-87064705	K562	blood:	n/a	n/a
7	ATF1	chr2:87046445-87047301	K562	blood:	n/a	n/a
8	ATF1	chr2:87008495-87009694	K562	blood:	n/a	n/a
9	ATF1	chr2:86991865-86992162	K562	blood:	n/a	n/a
10	ATF1	chr2:87056647-87057105	K562	blood:	n/a	n/a
11	ATF2	chr2:87011024-87011666	GM12878	blood:	n/a	n/a
12	ATF2	chr2:87011061-87011568	GM12878	blood:	n/a	n/a
13	ATF3	chr2:87035407-87035871	A549	lung:	n/a	n/a
14	ATF3	chr2:86975156-86975457	K562	blood:	n/a	n/a
15	ATF3	chr2:87035386-87035875	A549	lung:	n/a	n/a
16	BACH1	chr2:87013427-87013719	K562	blood:	n/a	n/a
17	BACH1	chr2:87059079-87059327	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr2:87017296-87017709	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr2:87035036-87035962	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr2:87011135-87011439	GM12878	blood:	n/a	n/a
21	BATF	chr2:87067239-87067491	GM12878	blood:	n/a	n/a
22	BATF	chr2:87011070-87011355	GM12878	blood:	n/a	n/a
23	BCL11A	chr2:87067184-87067494	GM12878	blood:	n/a	n/a
24	BCL11A	chr2:87067240-87067563	GM12878	blood:	n/a	n/a
25	BCLAF1	chr2:87035400-87035852	GM12878	blood:	n/a	chr2:87035834-87035847
26	BCLAF1	chr2:87011028-87011445	GM12878	blood:	n/a	n/a
27	BCLAF1	chr2:87035432-87035863	GM12878	blood:	n/a	chr2:87035834-87035847
28	BHLHE40	chr2:87005690-87005862	K562	blood:	n/a	n/a
29	BHLHE40	chr2:87034191-87035985	HepG2	liver:	n/a	n/a
30	BHLHE40	chr2:87062031-87062296	K562	blood:	n/a	n/a
31	BHLHE40	chr2:87012885-87013701	K562	blood:	n/a	n/a
32	BHLHE40	chr2:87035462-87036013	GM12878	blood:	n/a	n/a
33	BHLHE40	chr2:87035439-87036253	K562	blood:	n/a	n/a
34	BHLHE40	chr2:87056607-87056890	K562	blood:	n/a	n/a
35	BHLHE40	chr2:87051039-87051340	K562	blood:	n/a	n/a
36	BHLHE40	chr2:87007042-87007239	K562	blood:	n/a	n/a
37	BHLHE40	chr2:87064342-87064452	K562	blood:	n/a	n/a
38	BRCA1	chr2:87034355-87036171	HepG2	liver:	n/a	n/a
39	BRCA1	chr2:87035437-87036065	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr2:87003606-87004881	HepG2	liver:	n/a	n/a
41	BRCA1	chr2:87064342-87064609	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr2:87048502-87048716	GM12878	blood:	n/a	n/a
43	BRCA1	chr2:87020513-87021352	HepG2	liver:	n/a	n/a
44	BRCA1	chr2:87028182-87028284	GM12878	blood:	n/a	n/a
45	BRCA1	chr2:87052250-87052793	HepG2	liver:	n/a	n/a
46	BRCA1	chr2:87059602-87059802	HepG2	liver:	n/a	chr2:87059766-87059773
47	CBX3	chr2:86977299-86977808	K562	blood:	n/a	n/a
48	CBX3	chr2:86977303-86977904	HCT-116	colon:	n/a	n/a
49	CBX3	chr2:86977251-86977767	K562	blood:	n/a	n/a
50	CBX3	chr2:86977325-86977792	HCT-116	colon:	n/a	n/a

(count:3120 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:87019846-87019896	Jurkat	blood:	n/a
2	chr2:87014979-87015029	CMK	blood:	n/a
3	chr2:87035698-87035748	Caco-2	colon:	n/a
4	chr2:87034800-87034850	HIPEpiC	eye:	n/a
5	chr2:87019192-87019242	PANC-1	pancreas:	n/a
6	chr2:87035710-87035760	ECC-1	luminal epithelium:	n/a
7	chr2:87020937-87020987	HCT-116	colon:	n/a
8	chr2:87052406-87052456	HCT-116	colon:	n/a
9	chr2:87036626-87036676	LNCaP	prostate:	n/a
10	chr2:87019846-87019896	Jurkat	blood:	n/a
11	chr2:87014979-87015029	CMK	blood:	n/a
12	chr2:87035698-87035748	Caco-2	colon:	n/a
13	chr2:87034800-87034850	HIPEpiC	eye:	n/a
14	chr2:87019192-87019242	PANC-1	pancreas:	n/a
15	chr2:87035710-87035760	ECC-1	luminal epithelium:	n/a
16	chr2:87020937-87020987	HCT-116	colon:	n/a
17	chr2:87052406-87052456	HCT-116	colon:	n/a
18	chr2:87036626-87036676	LNCaP	prostate:	n/a
19	chr2:87017591-87017641	AG09309	skin:	n/a
20	chr2:87018104-87018154	K562	blood:	n/a
21	chr2:87017591-87017641	GM06990	blood:	n/a
22	chr2:87048747-87048797	LNCaP	prostate:	n/a
23	chr2:87016436-87016486	BJ	skin:	n/a
24	chr2:87018054-87018104	HUVEC	blood vessel:	n/a
25	chr2:87035278-87035328	BE2_C	brain:	n/a
26	chr2:87034831-87034881	HL-60	blood:	n/a
27	chr2:87017953-87018003	PFSK-1	brain:	n/a
28	chr2:87040878-87040928	HCF	heart:	n/a
29	chr2:87035278-87035328	AoSMC	blood vessel:	n/a
30	chr2:87018958-87019008	NH-A	brain:	n/a
31	chr2:87035609-87035659	U87	brain:	n/a
32	chr2:87037000-87037050	GM12891	blood:	n/a
33	chr2:87059202-87059252	GM12878	blood:	n/a
34	chr2:87035278-87035328	HCPEpiC	choroid plexus:	n/a
35	chr2:87019612-87019662	HRPEpiC	eye:	n/a
36	chr2:87035688-87035738	SK-N-MC	brain:	n/a
37	chr2:87014979-87015029	H1-hESC	embryonic stem cell:	embryo
38	chr2:87034800-87034850	ovcar-3	ovarian:	n/a
39	chr2:87017689-87017739	HCF	heart:	n/a
40	chr2:87016436-87016486	GM12891	blood:	n/a
41	chr2:87034831-87034881	CMK	blood:	n/a
42	chr2:87016436-87016486	HRCEpiC	kidney:	n/a
43	chr2:87018966-87019016	NH-A	brain:	n/a
44	chr2:87034200-87034250	HUVEC	blood vessel:	n/a
45	chr2:87037000-87037050	GM12892	blood:	n/a
46	chr2:87035698-87035748	AG09309	skin:	n/a
47	chr2:87048489-87048539	AoSMC	blood vessel:	n/a
48	chr2:87035698-87035748	IMR90	lung:	fetal
49	chr2:87035278-87035328	AG09319	gingival:	n/a
50	chr2:87048747-87048797	AG09309	skin:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:86976811..86978782-chr2:86981681..86983709,3	K562	blood:
2	chr2:86972255..86973795-chr2:86976969..86979051,2	K562	blood:
3	chr2:86970428..86972701-chr2:86973505..86975478,2	MCF-7	breast:
4	chr2:87010879..87013037-chr2:87016931..87018584,2	MCF-7	breast:
5	chr2:86995678..86997239-chr2:87001923..87004036,2	K562	blood:
6	chr2:86850257..86852408-chr2:86970682..86973822,3	MCF-7	breast:
7	chr2:87004183..87006528-chr2:87007653..87009681,2	K562	blood:
8	chr2:86976092..86977901-chr2:86986251..86989473,3	K562	blood:
9	chr2:87030047..87032736-chr2:87033123..87034744,3	MCF-7	breast:
10	chr2:86972255..86973795-chr2:86976969..86979051,2	K562	blood:
11	chr2:86991045..86994213-chr2:86994492..86997547,4	K562	blood:
12	chr2:87035298..87037035-chr2:87037234..87038983,2	MCF-7	breast:
13	chr2:87030047..87032736-chr2:87033123..87034744,3	MCF-7	breast:
14	chr2:86995678..86997239-chr2:87001923..87004036,2	K562	blood:
15	chr2:86992690..86995505-chr2:86996197..86998560,2	MCF-7	breast:
16	chr2:87053953..87055906-chr2:87062095..87066104,3	MCF-7	breast:
17	chr2:87027429..87029598-chr2:87032662..87035467,2	MCF-7	breast:
18	chr2:87016632..87018790-chr2:87032170..87034818,2	MCF-7	breast:
19	chr2:86986605..86989075-chr2:86997944..86999787,2	K562	blood:
20	chr2:86991626..86993002-chr2:87034779..87035758,6	MCF-7	breast:
21	chr2:86991626..86993002-chr2:87034779..87035758,6	MCF-7	breast:
22	chr2:87004183..87006528-chr2:87007653..87009681,2	K562	blood:
23	chr2:87029729..87031828-chr2:87033631..87036000,2	K562	blood:
24	chr2:87002968..87006528-chr2:87006846..87010010,3	K562	blood:
25	chr2:87006827..87008386-chr2:87009565..87012245,2	K562	blood:
26	chr2:86850136..86852379-chr2:86973884..86976847,2	K562	blood:
27	chr2:86975250..86978690-chr2:86981648..86984537,4	K562	blood:
28	chr2:86623288..86624016-chr2:87035607..87036117,2	K562	blood:
29	chr2:86976092..86977901-chr2:86986251..86989473,3	K562	blood:
30	chr2:86666465..86668622-chr2:86979172..86981000,2	K562	blood:
31	chr2:87027429..87029598-chr2:87032662..87035467,2	MCF-7	breast:
32	chr2:87053953..87055906-chr2:87062095..87066104,3	MCF-7	breast:
33	chr2:86976811..86978782-chr2:86981681..86983709,3	K562	blood:
34	chr2:87006827..87008386-chr2:87009565..87012245,2	K562	blood:
35	chr2:86932548..86934420-chr2:86983184..86985125,2	MCF-7	breast:
36	chr2:86849445..86851190-chr2:87032691..87035125,2	MCF-7	breast:
37	chr2:87002968..87006528-chr2:87006846..87010010,3	K562	blood:
38	chr2:86997290..86998210-chr2:87035221..87035730,2	MCF-7	breast:
39	chr2:87037113..87040779-chr2:87041789..87043828,3	MCF-7	breast:
40	chr2:87046936..87049292-chr2:87052783..87055158,2	K562	blood:
41	chr2:87009642..87012504-chr2:87015685..87018446,2	MCF-7	breast:
42	chr2:87037113..87040779-chr2:87041789..87043828,3	MCF-7	breast:
43	chr2:87046936..87049292-chr2:87052783..87055158,2	K562	blood:

No data

(count:9 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	RMND5A	hsa-miR-27a-3p	chr2:87001620-87001627
2	RMND5A	hsa-miR-27a-3p	chr2:87004202-87004222
3	RMND5A	hsa-miR-21-5p	chr2:87000639-87000646
4	RMND5A	hsa-miR-128-3p	chr2:87001679-87001699
5	RMND5A	hsa-miR-27a-3p	chr2:87002320-87002339
6	RMND5A	hsa-miR-125b-5p	chr2:87004984-87004990
7	RMND5A	hsa-miR-27a-3p	chr2:87001607-87001627
8	RMND5A	hsa-miR-21-5p	chr2:87000626-87000646
9	RMND5A	hsa-miR-23b-3p	chr2:87002901-87002921

Variant related genes	Relation type
CD8A	TF binding region
RMND5A	TF binding region
CD8A	CpG island
RMND5A	CpG island
ENSG00000115548	chromatin interactions
ENSG00000239305	chromatin interactions
ENSG00000249884	chromatin interactions
ENSG00000153561	chromatin interactions
ENSG00000153563	chromatin interactions

Extended variants
information (count: 3727 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:3727 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374637485	chr2:86961459-86961460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs370163773	chr2:86961493-86961494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs541068120	chr2:86961501-86961502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs374445135	chr2:86961512-86961513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559076669	chr2:86961529-86961530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs62148502	chr2:86961602-86961603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs530982821	chr2:86961722-86961723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs578202887	chr2:86961799-86961800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs72624654	chr2:86961902-86961903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs563562660	chr2:86962136-86962137	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs62148503	chr2:86962152-86962153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2944256	chr2:86962184-86962185	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549150769	chr2:86962194-86962195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561462493	chr2:86962229-86962230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs201599938	chr2:86962230-86962231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547015676	chr2:86962288-86962289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs376926106	chr2:86962535-86962536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571513451	chr2:86962542-86962543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533270776	chr2:86962558-86962559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560392335	chr2:86962674-86962675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs2674792	chr2:86963313-86963314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs2612961	chr2:86963376-86963377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs551664885	chr2:86963480-86963481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs2612968	chr2:86963591-86963592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs200045676	chr2:86963608-86963609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569947870	chr2:86963855-86963856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537268804	chr2:86963860-86963861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547733830	chr2:86963862-86963863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs199549319	chr2:86963871-86963872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs112274026	chr2:86964263-86964264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs377580166	chr2:86964698-86964699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538822304	chr2:86964700-86964701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200095226	chr2:86964809-86964810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371304384	chr2:86965082-86965083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375912534	chr2:86965415-86965416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534379240	chr2:86965637-86965638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs552934817	chr2:86965653-86965654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs554704122	chr2:86965711-86965712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577539720	chr2:86966075-86966076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs71411865	chr2:86966078-86966079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2203524	chr2:86966527-86966528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs2203525	chr2:86966608-86966609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs62148504	chr2:86966641-86966642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs62148505	chr2:86967028-86967029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs62148506	chr2:86967046-86967047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201857768	chr2:86967398-86967399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545311608	chr2:86967459-86967460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201987371	chr2:86967568-86967569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575511072	chr2:86967689-86967690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs542862550	chr2:86967827-86967828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	18438408	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	16272173	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	19812545	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:3061 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:86948800-86972600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr2:86949000-86970200	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr2:86949000-86970200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr2:86949000-86970200	Weak transcription	Fetal Intestine Small	intestine
5	chr2:86949000-86979600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr2:86951400-86970200	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr2:86956400-86963400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr2:86956400-86970400	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr2:86956800-86971200	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr2:86959600-86969800	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr2:86961400-86961600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
12	chr2:86961600-86971200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr2:86962000-86962200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr2:86962000-86962200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr2:86962200-86975400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr2:86962200-86977000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr2:86963200-86963400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr2:86963400-86963600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
19	chr2:86963400-86963600	Enhancers	Fetal Thymus	thymus
20	chr2:86963600-86969200	Weak transcription	Fetal Thymus	thymus
21	chr2:86963600-86972400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr2:86965200-86978800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr2:86966200-86970200	Weak transcription	Fetal Intestine Large	intestine
24	chr2:86966600-86970200	Weak transcription	Duodenum Mucosa	Duodenum
25	chr2:86966800-86970800	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr2:86966800-86977200	Weak transcription	Osteobl	bone
27	chr2:86967000-86970200	Weak transcription	HepG2	liver
28	chr2:86967000-86971200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr2:86967400-86969800	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr2:86967400-86970200	Weak transcription	Primary B cells from peripheral blood	blood
31	chr2:86967600-86969800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr2:86967600-86969800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr2:86967600-86970200	Weak transcription	Dnd41	blood
34	chr2:86967600-86971400	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr2:86967800-86970600	Weak transcription	Fetal Muscle Leg	muscle
36	chr2:86968000-86968200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr2:86968000-86968200	Enhancers	Liver	Liver
38	chr2:86968000-86971200	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr2:86968200-86970000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr2:86968200-86970000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr2:86968200-86970000	Weak transcription	Thymus	Thymus
42	chr2:86968200-86971200	Weak transcription	Liver	Liver
43	chr2:86968400-86970000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr2:86968400-86970000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr2:86968400-86970000	Weak transcription	Fetal Muscle Trunk	muscle
46	chr2:86968400-86970000	Weak transcription	Fetal Stomach	stomach
47	chr2:86968400-86970200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr2:86968400-86970200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr2:86968600-86970000	Weak transcription	A549	lung
50	chr2:86968600-86970200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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